The uncertainty in the position of mobile organs during radiotherapy limits the accuracy of treatment. Therefore several groups developed image guidance methods for correction of the target position using markers, ultrasound, and in-room CT. Recently, we integrated a cone-beam CT on a linear accelerator (Elekta Synergy Research Platform) in our hospital. The purpose of this paper is to present our first clinical experience, evaluating dose, image quality, and geometric accuracy in 28 patients. For a complete CT reconstruction, data are acquired over 30–250 s (80–700 projections), depending on the required image quality. The CT reconstruction (using in-house developed image guidance software) of a 256 × 256 × 256 volume (with 1 mm cubic voxel size) takes about 20 s. With a central detector position the field of view is 25 cm × 25 cm × 25 cm. Offsetting the detector by 11 cm increases the field of view to 40 cm × 40 cm × 25 cm. At the increased field of view a 360 degree gantry rotation is required, while for the smaller field of view about 190 degree gantry rotation suffices for a proper CT reconstruction. The dose was quantified using an ionization chamber inserted in a Rando-phantom. For quality assurance of the geometric accuracy and image quality studies, 140 cone-beam scans were made of 28 patients, mostly treated for prostate, head and neck, and lung cancer. The setup error was determined by automatically registering bony anatomy in the cone-beam CT scan to the planning CT scan, taking planning data (isocenter) into account. For all patients, setup errors determined with the cone beam system were compared with those determined using electronic portal images (of the same fraction) and DRRs. Automatic soft tissue registration for prostate has been implemented. Prostate calcifications were present in 3 patients, and were used as inherent markers to validate the prostate localization accuracy. The dose required to scan a head and neck patient with good image quality was 1 cGy (central) and 1.8 cGy skin dose. Doses for a pelvic patient were slightly lower. The image quality was sufficient to visualize soft tissues such as lung tumors, rectum, and bladder. The prostate was visible, but not in all slices. Scan truncation artifacts (because the patient shadow does not fit on the detector) caused Hounsfield unit calibration problems but hardly influenced image quality or image registration. The cone beam data clearly revealed setup error, as well as anatomical deformations due to neck flex and tumor regression. Comparison between cone beam data and portal image derived setup errors showed differences of about 1 mm SD for all three axis for head and neck and prostate. These differences were mainly attributed to observer variation in portal image analysis. In addition there was a systematic error of 1 mm in the cranio-caudal direction, caused by inherent inaccuracy of the MV isocenter. For lung cancer patients, the differences were around 3 mm SD, indicating a much larger observer variation in portal image analysis for this patient group. To evaluate patient motion and respiration differences between cone beam CT and portal images, DRRs made of cone-beam data were directly compared with the portal images. These differences were smaller than 1 mm. The accuracy of automatic prostate tracking using cone beam data was 1.7 mm SD (AP direction) and better in other directions. Our clinical validation showed that imaging dose and geometric accuracy compare favorable with electronic portal imaging. For this reason, electronic portal imaging has been replaced by cone-beam imaging on this accelerator since February 2004. At present, an off-line positioning protocol for bony anatomy setup is in clinical use. The next step is to implement soft-tissue based setup corrections clinically. Protocols for prostate (based on automatic prostate tracking) and lung (based on respiration correlated cone-beam CT) are in development
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